ABSTRACT
Collecting energy from the ubiquitous water cycle has emerged as a promising technology for power generation. Here, we have developed a sustainable moisture absorption-evaporation cycling fabric (Mac-fabric). On the basis of the cycling unidirectional moisture conduction in the fabric and charge separation induced by the negative charge channel, sustainable constant voltage power generation can be achieved. A single Mac-fabric can achieve a high power output of 0.144 W/m2 (5.76 × 102 W/m3) at 40% relative humidity (RH) and 20°C. By assembling 500 series and 300 parallel units of Mac-fabrics, a large-scale demo achieves 350 V of series voltage and 33.76 mA of parallel current at 25% RH and 20°C. Thousands of Mac-fabric units are sewn into a tent to directly power commercial electronic products such as mobile phones in outdoor environments. The lightweight (300 g/m2) and soft characteristics of the Mac-fabric make it ideal for large-area integration and energy collection in real circumstances.
ABSTRACT
Electronic textiles have gradually evolved into one of the most important mainstays of flexible electronics owing to their good wearability. However, textile multifunctionality is generally achieved by stacking functional modules, which is not conducive to wearability. Integrating these modules into a single fiber provides a better solution. In this work, a core-spun functional fiber (CSF) constructed from hyper-environmentally stable Zn-based eutectogel as the core layer and polytetrafluoroethylene as the sheath is designed. The CSF achieves a synergistic output effect of piezoelectricity-enhanced triboelectricity, as well as reliable hydrophobicity, and high mid-infrared emissivity and visible light reflectivity. A monolayer functionalized integrated textile is woven from the CSF to enable effective energy (mechanical and droplet energy) harvesting and personal thermal management functions. Furthermore, scenarios for the energy supply, motion detection, and outdoor use of electronic fabrics for electronics applications are demonstrated, opening new avenues for the functional integration of electronic textiles.
ABSTRACT
We have demonstrated, for the first time, high-efficient non-destructive and non-derivative dissolution of cellulose could be achieved in cryogenic aqueous phosphoric acid. Cellulose from different sources and of varying degree of polymerization from 200 (MCC) to 2200 (cotton fabric) could be dissolved completely to afford solutions containing 5 wt%-18 wt% cellulose, from which ultra-strong and tough cellulose films of tensile strength as high as 707 MPa could be obtained using water as the coagulant. These solutions can be stored at -18 °C for extended time without noticeable degradation while desired degree of polymerization is also attainable by tuning the storage conditions. The findings of this work call for renewal attention on phosphoric acid as a promising cellulose solvent for being non-toxic, non-volatile, easy to handle, and cost-effective.
ABSTRACT
Aiming at recyclable catalyst carriers, porous cellulose macrospheres from wood pulp dissolved in an alkaline urea system were regenerated by simple injection regeneration. After solvent exchange, porous cellulose macrospheres (CMs) with a high specific surface area of 325.3 m2 g-1 were obtained by lyophilization, and CuS nanoparticles (CuS NPs) were coated on CMs by in situ growth in the liquid phase to achieve CuS-supported CM macrospheres (CuS@CM). The results indicated that the CuS@CM biocatalyst was successfully prepared with an average diameter of approximately 1.2 mm. In addition, CuS@CM was further used as a heterogeneous catalyst for the catalytic degradation of methylene blue (MB) and methyl orange (MO) model dyes during the oxidation of hydrogen peroxide (H2O2). In the presence of low doses of H2O2, the degradation rate of MB reached 94.8% within 10 min, showing high catalytic activity under neutral and alkaline conditions. After five cycles, 90.1% of the original catalytic activity was still retained, indicating that the prepared CuS@CM composite possessed excellent catalytic activity and reusability.
